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SRPS EN ISO 15223-1:2022

Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements (ISO 15223-1:2021)

Dec 30, 2022

General information

60.60     Dec 30, 2022

ISS

Z210

European Norm

01.080.20     11.040.01  

English  

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Published

Language in which you want to receive the document.

Scope

This document specifies symbols used to express information supplied for a medical device. This document is applicable to symbols used in a broad spectrum of medical devices, that are available globally and need to meet different regulatory requirements.
These symbols can be used on the medical device itself, on its packaging or in the accompanying information. The requirements of this document are not intended to apply to symbols specified in other standards.

Related directives

Directives related to this standard.

2017/745

Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC

Harmonized
2017/746

Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU

Harmonized

Life cycle

PREVIOUSLY

WITHDRAWN
SRPS EN ISO 15223-1:2017

NOW

PUBLISHED
SRPS EN ISO 15223-1:2022
60.60 Standard published
Dec 30, 2022

Related project

Adopted from EN ISO 15223-1:2021

Adopted from ISO 15223-1:2021